[Complete congenital heart block. Its natural history and evolution].

F Millán, E Becker, P Iturralde, A Arteaga, A Medeiros, L Colín, J A González Hermosillo
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Abstract

This study describes the natural history and evolution of 67 patients with congenital auriculoventricular heart block admitted in the Instituto Nacional de Cardiología "Ignacio Chávez", Mexico, D.F. from 1944 to 1998. There were 35 (52%) females and 32 (47%) males, with mean follow up period of 93.7 +/- 104 months. Most of the patients were without structural cardiovascular disease (90%). The most frequent symptoms were dyspnea and syncope. Electrocardiograms showed a ventricular heart rate of 42.2 +/- 9 beats/minute. 85.7% of patients had a supra-Hisian complete heart block. In 31% of patients a pacemaker was implanted because syncope. Overall mortality was 4.4% and malignant ventricular arrhythmias were the principal contributors. Risk factors for mortality identified in this study were junctional escape rhythm lower than 50 beats/minute, inappropriate chronotropic response during exercise, R-R interval prolongation at night, enlargement of cardiac chambers, depressed left ventricular ejection fraction and prolonged QT interval. In all of these conditions we recommend permanent pacemaker implantation.

完全性先天性心脏传导阻滞。它的自然历史和进化]。
本研究描述了1944年至1998年在墨西哥国立医院Cardiología“伊格纳西奥Chávez”收治的67例先天性耳室传导阻滞患者的自然历史和演变。女性35例(52%),男性32例(47%),平均随访时间93.7±104个月。大多数患者无结构性心血管疾病(90%)。最常见的症状是呼吸困难和晕厥。心电图显示心室心率为42.2±9次/分钟。85.7%的患者有超希氏完全性心脏传导阻滞。31%的患者因为晕厥而植入心脏起搏器。总死亡率为4.4%,恶性室性心律失常是主要原因。本研究确定的死亡危险因素为结期逃逸节律低于50次/分钟、运动时不适当的变时反应、夜间R-R间期延长、心腔增大、左室射血分数降低和QT间期延长。在所有这些情况下,我们建议植入永久性起搏器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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